p-Terphenyl - CAS 92-94-4
Catalog: |
BB040722 |
Product Name: |
p-Terphenyl |
CAS: |
92-94-4 |
Synonyms: |
1,4-diphenylbenzene |
Application: |
Terphenyl mixtures are used as heat transfer media, dye carriers, and in the production of lubricants. |
IUPAC Name: | 1,4-diphenylbenzene |
Description: | p-Terphenyl is a detector of neutron. It can be used in analytical studies. |
Molecular Weight: | 230.30 |
Molecular Formula: | C18H14 |
Canonical SMILES: | C1=CC=C(C=C1)C2=CC=C(C=C2)C3=CC=CC=C3 |
InChI: | InChI=1S/C18H14/c1-3-7-15(8-4-1)17-11-13-18(14-12-17)16-9-5-2-6-10-16/h1-14H |
InChI Key: | XJKSTNDFUHDPQJ-UHFFFAOYSA-N |
Boiling Point: | 383 °C |
Melting Point: | 210 °C - 214 °C |
Flash Point: | 405 °F |
Purity: | 98% |
Density: | 1.23 g/cm3 |
Solubility: | Insoluble |
Appearance: | White to off-white solid |
Storage: | RT. Keep in the tight container. |
MDL: | MFCD00003061 |
LogP: | 5.02060 |
Vapor Pressure: | Very low (NIOSH, 2022) |
GHS Hazard Statement: | H315 (97.96%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P391, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113341452-A | Process flow for manufacturing nuclear detection beta scintillator | 20210531 |
CN-113214056-A | Biphenyl compound and diterpenoid compound as well as preparation method and application thereof | 20210416 |
KR-20210035161-A | A process for producing polyetherketoneketone mixed resin composition and polyetherketoneketone thereof | 20210325 |
CN-113185628-A | Polystyrene scintillation microsphere and preparation method thereof | 20210322 |
CN-113066972-A | Lithium-supplementing silicon material, preparation method thereof, electrode containing lithium-supplementing silicon material and battery | 20210319 |
PMID | Publication Date | Title | Journal |
27725436 | 20160101 | Ligand Activity of Group 15 Compounds Possessing Triphenyl Substituent for the RXR and PPARγ Nuclear Receptors | Biological & pharmaceutical bulletin |
23441911 | 20130327 | Isolation and characterization of new p-Terphenyls with antifungal, antibacterial, and antioxidant activities from halophilic actinomycete Nocardiopsis gilva YIM 90087 | Journal of agricultural and food chemistry |
23040979 | 20121109 | Synthesis of polychlorinated terphenyl mixtures and gas chromatography with mass spectrometry data of tetra- to octachlorinated ortho-, meta-, and para-terphenyls | Journal of chromatography. A |
23061916 | 20121102 | Phenyl shifts in substituted arenes via ipso arenium ions | The Journal of organic chemistry |
22996418 | 20121022 | Efficient synthesis of oxygenated terphenyls and other oligomers: sequential arylation reactions through phenol oxidation-rearomatization | Chemistry (Weinheim an der Bergstrasse, Germany) |
Complexity: | 198 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 230.109550447 |
Formal Charge: | 0 |
Heavy Atom Count: | 18 |
Hydrogen Bond Acceptor Count: | 0 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 230.109550447 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 0 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 5.6 |
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